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nsv2734612

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,869

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 423 SVs from 40 studies. See in: genome view    
Remapped(Score: Perfect):7,505,902-7,516,770Question Mark
Overlapping variant regions from other studies: 21 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):91,721-102,589Question Mark
Overlapping variant regions from other studies: 427 SVs from 40 studies. See in: genome view    
Remapped(Score: Perfect):7,505,902-7,516,770Question Mark
Overlapping variant regions from other studies: 12 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):91,721-102,589Question Mark
Overlapping variant regions from other studies: 240 SVs from 15 studies. See in: genome view    
Submitted genomic7,495,902-7,506,770Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv2734612RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr97,505,9027,516,770
nsv2734612RemappedPerfectGRCh38.p12ALT_REF_LOCI_1Second PassNW_003315928.1Chr9|NW_00
3315928.1		91,721102,589
nsv2734612RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr97,505,9027,516,770
nsv2734612RemappedPerfectGRCh37.p13PATCHESSecond PassNW_003315928.1Chr9|NW_00
3315928.1		91,721102,589
nsv2734612Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000009.10Chr97,495,9027,506,770

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13612564deletionSNP arrayProbe signal intensity
nssv13616777deletionSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv13612564RemappedPerfectNW_003315928.1:g.(
?_91721)_(102589_?
)del		GRCh38.p12Second PassNW_003315928.1Chr9|NW_00
3315928.1		91,721102,589
nssv13616777RemappedPerfectNW_003315928.1:g.(
?_91721)_(102589_?
)del		GRCh38.p12Second PassNW_003315928.1Chr9|NW_00
3315928.1		91,721102,589
nssv13612564RemappedPerfectNC_000009.12:g.(?_
7505902)_(7516770_
?)del		GRCh38.p12First PassNC_000009.12Chr97,505,9027,516,770
nssv13616777RemappedPerfectNC_000009.12:g.(?_
7505902)_(7516770_
?)del		GRCh38.p12First PassNC_000009.12Chr97,505,9027,516,770
nssv13612564RemappedPerfectNW_003315928.1:g.(
?_91721)_(102589_?
)del		GRCh37.p13Second PassNW_003315928.1Chr9|NW_00
3315928.1		91,721102,589
nssv13616777RemappedPerfectNW_003315928.1:g.(
?_91721)_(102589_?
)del		GRCh37.p13Second PassNW_003315928.1Chr9|NW_00
3315928.1		91,721102,589
nssv13612564RemappedPerfectNC_000009.11:g.(?_
7505902)_(7516770_
?)del		GRCh37.p13First PassNC_000009.11Chr97,505,9027,516,770
nssv13616777RemappedPerfectNC_000009.11:g.(?_
7505902)_(7516770_
?)del		GRCh37.p13First PassNC_000009.11Chr97,505,9027,516,770
nssv13612564Submitted genomicNC_000009.10:g.(?_
7495902)_(7506770_
?)del		NCBI36 (hg18)NC_000009.10Chr97,495,9027,506,770
nssv13616777Submitted genomicNC_000009.10:g.(?_
7495902)_(7506770_
?)del		NCBI36 (hg18)NC_000009.10Chr97,495,9027,506,770

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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